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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1486701Erstellt: 25. Oktober 2026

Dichloromethane → 1-(4-Amino-pyrimidin-2-ylmethyl)-piperidine-4-carboxylic acid tert-butylamide

https://huagongshe.com/reaction/1486701

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktSodium HydroxideHCID 14798—
EduktN-tert-butylpiperidine-4-carboxamideHCID 7175833—
Edukt2-(Chloromethyl)pyrimidin-4-amineHCID 21298827—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produkt1-(4-Amino-pyrimidin-2-ylmethyl)-piperidine-4-carboxylic acid tert-butylamideHCID 8670653394%

Reaktionsschritte

A solution of 2-chloromethyl-pyrimidin-4-ylamine (Imperial Chemical Industries PLC Patent: U.S. Pat. No. 4,447,441 A1, 1984; 300 mg, 2.1 mmol) in methanol (25 mL) is treated with piperidine-4-carboxylic acid tert-butylamide (404 mg, 2.19 mmol) and TEA (0.872 mL, 6.27 mmol). The resulting mixture is heated at reflux overnight. DCM (25 mL) and water (25 mL) are added followed by NaOH 1M to adjust at pH 10. The organic phase is separated. The aqueous phase is extracted with DCM (25 mL). The combined organic phases are dried over MgSO4, filtered and evaporated. Evaporation of the solvent yields the crude product (0.57 g, 94%) as a brownish solid; LC-MS A: tR=0.40 min; [M+H]+=292.14.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09428456B2
Quelldatensatzuspto-grants-2016_08
ORD IDord-db09b09acbf6436cb68efe04beeb0e7b
Quellennotizuspto-grants-2016_08